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The retinoblastoma protein/p16.

Authors :
Stankiewicz, Elzbieta
Prowse, David M.
Ktori, Elena
Cuzick, Jack
Ambroisine, Laurence
Xiaox Zhang
Kudahetti, Sakunthala
Watkin, Nicholas
Corbishley, Catherine
Berney, Daniel M.
Source :
Histopathology. Feb2011, Vol. 58 Issue 3, p433-439. 7p. 1 Color Photograph, 3 Charts.
Publication Year :
2011

Abstract

Stankiewicz E, Prowse D M, Ktori E, Cuzick J, Ambroisine L, Zhang X, Kudahetti S, Watkin N, Corbishley C & Berney D M (2011) Histopathology, 433-439 The pathogenesis of penile squamous cell carcinoma (PSCC) is not well understood. Human papillomavirus (HPV) may be involved in carcinogenesis, but few studies have compared cell-cycle protein expression in HPV positive and negative cancers. The aim was to determine the extent of HPV infection in different histological subtypes of PSCC and its impact on the expression of key cell-cycle proteins: p53, p21, p16 and retinoblastoma (RB) protein. One hundred and forty-eight PSCC samples were examined immunohistochemically for RB, p16, p53 and p21 protein expression. One hundred and two cases were typed for HPV by PCR. HPV DNA was detected in 56% of tumours, with HPV16 present in 81%. Basaloid tumours were related strongly to HPV infection (10 of 13), while verrucous were not (three of 13). Fifty-nine per cent (38 of 64) of usual type SCCs had HPV infection. RB protein correlated negatively ( P < 0.0001) and p16 ( P < 0.0001) and p21 ( P = 0.0002) correlated positively with HPV infection. p53 did not correlate with HPV infection. HPV infection is present in more than half of penile cancers and it is responsible for RB pathway disruption. However, no link between HPV and p53 immunodetection was found. Only basaloid and half of usual-type PSSCs correlate with HPV infection, confirming possible separate aetiologies for those tumours. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03090167
Volume :
58
Issue :
3
Database :
Academic Search Index
Journal :
Histopathology
Publication Type :
Academic Journal
Accession number :
58702367
Full Text :
https://doi.org/10.1111/j.1365-2559.2011.03762.x